Dong-Yeun Koh
Korea Advanced Institute of Science and Technology · Environmental Science
About the Lab
Professor Dong-Yeun Koh's research lab specializes in advanced materials and membrane technologies for sustainable energy and environmental applications. Key research directions include the development of carbon molecular sieve membranes for selective organic liquid separations, MXene-based hydrogels for durable and self-healing wearable sensors, and gas hydrate-based systems for methane recovery and carbon dioxide sequestration. The lab also investigates molecular-level interactions in clathrate hydrates for hydrogen storage and CO2 capture, emphasizing materials design for energy efficiency and environmental remediation.
Research Overview
Research Output Trend
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Selected Papers
15Liquid-phase separations of similarly sized organic molecules using membranes is a major challenge for energy-intensive industrial separation processes. We created free-standing carbon molecular sieve membranes that translate the advantages of reverse osmosis for aqueous separations to the separation of organic liquids. Polymer precursors were cross-linked with a one-pot technique that protected the porous morphology of the membranes from thermally induced structural rearrangement during carboni
Abstract Very recently, MXene‐based wearable hydrogels have emerged as promising candidates for epidermal sensors due to their tissue‐like softness and unique electrical and mechanical properties. However, it remains a challenge to achieve MXene‐based hydrogels with reliable sensing performance and prolonged service life, because MXene inevitably oxidizes in water‐containing system of the hydrogels. Herein, catechol‐functionalized poly(vinyl alcohol) (PVA‐CA)‐based hydrogels is proposed to inhib
The direct recovery of methane from massive methane hydrates (MHs), artificial MH-bearing clays, and natural MH-bearing sediments is demonstrated, using either CO(2) or a CO(2)/N(2) gas mixture (20 mol % of CO(2) and 80 mol % of N(2), reproducing flue gas from a power plant) for methane replacement in complex marine systems. Natural gas hydrates (NGHs) can be converted into CO(2) hydrate by a swapping mechanism. The overall process serves a dual purpose: it is a means of sustainable energy-sourc
CO2 absorption is a key to alleviating the environmental consequences of fossil fuel combustion, which is a major source of global CO2 emission. Membrane contactors have showcased several competitive advantages in CO2 absorption over conventional gas–liquid contactors (e.g., packed towers), such as a large mass-transfer area and a safe operation owing to the membranes that physically separate the gas and liquid phases. This Review discusses the state-of-the-art studies related to CO2 absorption
The direct recovery of methane from gas hydrate‐bearing sediments is demonstrated, where a gaseous mixture of CO 2 + N 2 is used to trigger a replacement reaction in complex phase surroundings. A one‐dimensional high‐pressure reactor (8 m) was designed to test the actual aspects of the replacement reaction occurring in natural gas hydrate (NGH) reservoir conditions. NGH can be converted into CO 2 hydrate by a “replacement mechanism,” which serves double duty as a means of both sustainable energy
As hydrogen molecules enter the clathrate hydrate body, the ubiquitous dodecahedral cavity (5 12 ) is too small to allow anything but single occupancy thermodynamically. The possibility that H 2 double occupancy can occur in the dodecahedral cavity has been suggested and is still under debate. Here we uncover the unique feature of multiple occupancy of the hydrogen molecule in a dodecahedral cavity as induced by tuning the cage dimensions. The guest promoter population in the hydrate matrix spon
Abstract Carbon molecular sieve (CMS) membranes are considered game-changers to overcome the challenges that conventional polymeric membranes face. However, CMS membranes also confront a challenge in successfully separating extremely similar-sized molecules. In this article, high-precision tuning of the microstructure of CMS membranes is proposed by controlled electron irradiation for the separation of molecules with size differences less than 0.05 nm. Fitting CMS membranes for targeted molecula
Metal-organic frameworks (MOFs) are a class of microporous materials that have been highlighted with fast and selective sorption of gas molecules; however, they are at least partially unstable in the scale-up process. Here, we report a rational shaping of MOFs in a scalable architecture of fiber sorbent. The long-standing stability challenge of MOFs was resolved by using stable metal oxide precursors that are subject to controlled surface oxide dissolution-growth chemistry during the Mg-based MO
We report a new concept of structural transformation combined with tuning phenomena which together result in a significant increase in the hydrogen storage capacity in an icy material. It is necessary to investigate the use of a fully water-soluble structure H (sH) former so as to observe how hydrogen molecules are stably loaded into hydrate cages.
While two-dimensional (2D) Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub> MXene in aqueous dispersions spontaneously oxidizes into titanium dioxide (TiO<sub>2</sub>) nanocrystals, the crystallization mechanism has not been comprehensively understood and the resultant crystal structures are not controlled among three representative polymorphs: anatase, rutile, and brookite. In this study, such control on the lattice structures and domain sizes of the MXene-derived TiO<sub>2</sub> crystallites is
Abstract Promising advances in membrane technology can lead to energy-saving and eco-friendly solutions in industrial sectors. This work demonstrates a highly selective membrane with ultrathin and highly interconnected organosiloxane polymer nanolayers by initiated chemical vapor deposition to effectively separate solutes within the molecular weight range of 150–300 g mol −1 . We optimize the poly(1,3,5,7-tetravinyl-1,3,5,7-tetramethylcyclotetrasiloxane) membrane by adjusting both the thickness
Membranes could reform the field of molecular separations by enabling new low energy manufacturing technologies. This review article discusses the current state of the art and the potential in the 2D-enabled membrane separation processes by highlighting emerging and existing areas in which robust 2D materials significantly impact the energy-efficient separation process. Analysis of 2D-enabled membrane classes and prospective materials for 2D-enabled membranes are also discussed with emphasis on
Research Areas
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